Oak Carolina, Inc. is one of 8705 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oak Carolina, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SENSITEX EXAMINATION GLOVE, GLOVE, OAKTEX EXAMINATION, GLOVE, PATIENT EXAMINATION, GLOVE, EXAMINATION, VINYL
3
Total
3
Cleared
0
Denied
Oak Carolina, Inc. has 3 FDA 510(k) cleared medical devices. Based in Stow, US.
Historical record: 3 cleared submissions from 1996 to 1998. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Oak Carolina, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oak Carolina, Inc.
3 devices